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Recruiting Phase 1 Interventional

A Trial to Test the Safety and Efficacy of TEV-53408 in Participants With Vitiligo

ClinicalTrials.gov ID: NCT06625177

Public ClinicalTrials.gov record NCT06625177. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 7, 2026, 11:53 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b, Open-Label Trial to Assess Safety and Exploratory Efficacy of TEV-53408 in Participants With Vitiligo

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the trial is to evaluate the safety of TEV-53408 when given as an under the skin injection to adults with vitiligo. Vitiligo is a condition where patches of skin lose color (pigment) and turn white.

Study identification

NCT ID
NCT06625177
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Enrollment
66 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 11, 2024 (Actual)
Primary completion
Apr 26, 2028 (Estimated)
Completion
Jan 31, 2029 (Estimated)
Last update posted
Oct 29, 2026

2024 – 2029

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Scottsdale Clinical Research Scottsdale Arizona 85260 Terminated
Burke Pharmaceutical Research Hot Springs Arkansas 71913 Recruiting
Center for Dermatology Clinical Research, Inc. Fremont California 94538 Recruiting
University of CA Irvine Irvine California 92617 Active, not recruiting
Pasadena Clinical Trials Pasadena California 91101 Active, not recruiting
Watson Therapeutics Inc. (WTI), USA Miramar Florida 33025 Recruiting
MetroMed Clinical Trials Chicago Illinois 60614 Active, not recruiting
DS Research of Kentucky Louisville Kentucky 40421 Recruiting
Hamzavi Dermatology Canton Michigan 48187 Recruiting
Oregon Dermatology and Research Center Portland Oregon 97210 Recruiting
Dermatology Treatment & Research Center Dallas Texas 75230 Recruiting
Center for Clinical Studies, LTD. LLP Webster Texas 77598 Active, not recruiting
Jordan Valley Dermatology South Jordan Utah 84095 Active, not recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06625177, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 29, 2026 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06625177 live on ClinicalTrials.gov.

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